Pulmonary Ultrasound in the Diagnosis of Acute Thoracic Syndrome in Vaso-occlusive Sickle Cell Crisis (ECHO-STA)
Primary Purpose
Sickle-Cell Disease Nos With Crisis
Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
pulmonary ultrasound
Sponsored by
About this trial
This is an interventional diagnostic trial for Sickle-Cell Disease Nos With Crisis
Eligibility Criteria
Inclusion Criteria:
- Age: ≥12 months and <18 years
- Has a major sickle cell disease whatever the genotype
- Admission to hospital for a febrile vaso-occlusive crisis (VOC) or not
- Evolving at home for less than 48h
- Concomitant treatment with hydroxycarbamide / hydroxyurea possible
- Signed consent
- Patients affiliated to a French social security scheme
Exclusion Criteria:
- Child presenting an acute thoracic syndrome (ATS) from the outset at the admission
- Child who presented an ATS in the month preceding the inclusion
- Child in regular transfusion program or child who has received a hematopoietic stem cell transplant
- Child hospitalized at least 5 times for VOC in the year preceding inclusion (psychic problems making difficult the evaluation of the pain)
- Child who has already been included in the study during a previous VOC (each child participates in the study only once)
- VOC evolving for more than 48 hours before admission to the emergency room
- Acute splenic sequestration crisis at admission
Sites / Locations
- Hôpital Antoine Béclère
- Centre Hospitalier Intercommunal CréteilRecruiting
- Hôpital Bicêtre
- Hôpital Armand Trousseau
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Children with sickle cell disease
Arm Description
Child from 12 months to 18 years old admitted for vaso-occlusive crisis
Outcomes
Primary Outcome Measures
Sensitivity of pulmonary ultrasound
Proportion of subjects with positive pulmonary ultrasound among those with a positive chest X-ray at time t with 95% confidence interval at day 1
Sensitivity of pulmonary ultrasound
Proportion of subjects with positive pulmonary ultrasound among those with a positive chest X-ray at time t with 95% confidence interval at day 2
Sensitivity of pulmonary ultrasound
Proportion of subjects with positive pulmonary ultrasound among those with a positive chest X-ray at time t with 95% confidence interval at day 3
Secondary Outcome Measures
Specificity of pulmonary ultrasound
Proportion of subjects with a positive pulmonary ultrasound among those with a negative chest X-ray at time t at day 1
Specificity of pulmonary ultrasound
Proportion of subjects with a positive pulmonary ultrasound among those with a negative chest X-ray at time t at day 2
Specificity of pulmonary ultrasound
Proportion of subjects with a positive pulmonary ultrasound among those with a negative chest X-ray at time t at day 3
Sensitivity of pulmonary ultrasound in relation with ATS diagnosis
Proportion of subjects with positive pulmonary ultrasound among those with a positive chest X-ray at time t with 95% confidence intervalat day -3 of ATS diagnosis
Sensitivity of pulmonary ultrasound in relation with ATS diagnosis
Proportion of subjects with positive pulmonary ultrasound among those with a positive chest X-ray at time t with 95% confidence interval at day -1 of ATS diagnosis
Sensitivity of pulmonary ultrasound in relation with ATS diagnosis
Proportion of subjects with positive pulmonary ultrasound among those with a positive chest X-ray at time t with 95% confidence interval at day -2 of ATS diagnosis
Specificity of pulmonary ultrasound in relation with ATS diagnosis
Proportion of subjects with a positive pulmonary ultrasound among those with a negative chest X-ray at time t at day -1 of ATS diagnosis
Specificity of pulmonary ultrasound in relation with ATS diagnosis
Proportion of subjects with a positive pulmonary ultrasound among those with a negative chest X-ray at time t at day -3 of ATS diagnosis
Specificity of pulmonary ultrasound in relation with ATS diagnosis
Proportion of subjects with a positive pulmonary ultrasound among those with a negative chest X-ray at time t at day -2 of ATS diagnosis
Full Information
NCT ID
NCT03971136
First Posted
May 23, 2019
Last Updated
February 7, 2023
Sponsor
Centre Hospitalier Intercommunal Creteil
1. Study Identification
Unique Protocol Identification Number
NCT03971136
Brief Title
Pulmonary Ultrasound in the Diagnosis of Acute Thoracic Syndrome in Vaso-occlusive Sickle Cell Crisis
Acronym
ECHO-STA
Official Title
Evaluation of the Interest of Pulmonary Ultrasound in the Diagnosis and Early Detection of Acute Thoracic Syndrome in Hospitalized Children for Vaso-occlusive Sickle Cell Crisis: Multicenter Prospective Study
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 4, 2019 (Actual)
Primary Completion Date
April 30, 2023 (Anticipated)
Study Completion Date
July 1, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Intercommunal Creteil
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
ATS (acute thoracic syndrome) refers to acute pulmonary involvement in a sickle cell patient. The diagnosis is based on the association of clinical signs (fever or respiratory symptoms) with a recent pulmonary infiltrate on the chest x-ray.
The main objective of the study is to evaluate the place of the pulmonary ultrasound for the diagnosis of ATS, in comparison with frontal chest x-ray.
Detailed Description
The ATS occurs in half of the cases during hospitalization for a VOC (Vaso Occlusive crisis). The morbidity of ATS is important (respiratory insufficiency, duration of hospitalization, stays in intensive care, brain complications, pain, hypoxia, long-term sequelae, etc.) but no study has shown the benefits of curative treatments such as transfusion ( recommended at the time of diagnosis and practiced by some teams) or noninvasive ventilation (practiced by other teams). The first step before studying curative treatments is to have tools for early detection of ATS. Recent studies show non-inferiority of pulmonary ultrasonography compared to radiography and thoracic computed tomography in the diagnosis of pulmonary condensation (in adults and children). In a study performed in sickle cell adults admitted for ATS, pulmonary ultrasound was more sensitive than X-ray in detecting images of pulmonary consolidations visible on the chest CT scan.
Daswani et al have also shown the value of pulmonary ultrasound in comparison with radiography in the detection of consolidation lesions, suggestive of STA, in febrile children or young adults with sickle cell disease. They showed a good sensitivity (87%) and specificity (94%) of the pulmonary ultrasound.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sickle-Cell Disease Nos With Crisis
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
150 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Children with sickle cell disease
Arm Type
Other
Arm Description
Child from 12 months to 18 years old admitted for vaso-occlusive crisis
Intervention Type
Diagnostic Test
Intervention Name(s)
pulmonary ultrasound
Intervention Description
The subjects will have an ultrasound on admission and on day 1, 2 and 3
Primary Outcome Measure Information:
Title
Sensitivity of pulmonary ultrasound
Description
Proportion of subjects with positive pulmonary ultrasound among those with a positive chest X-ray at time t with 95% confidence interval at day 1
Time Frame
Day 1
Title
Sensitivity of pulmonary ultrasound
Description
Proportion of subjects with positive pulmonary ultrasound among those with a positive chest X-ray at time t with 95% confidence interval at day 2
Time Frame
Day 2
Title
Sensitivity of pulmonary ultrasound
Description
Proportion of subjects with positive pulmonary ultrasound among those with a positive chest X-ray at time t with 95% confidence interval at day 3
Time Frame
Day 3
Secondary Outcome Measure Information:
Title
Specificity of pulmonary ultrasound
Description
Proportion of subjects with a positive pulmonary ultrasound among those with a negative chest X-ray at time t at day 1
Time Frame
Day 1
Title
Specificity of pulmonary ultrasound
Description
Proportion of subjects with a positive pulmonary ultrasound among those with a negative chest X-ray at time t at day 2
Time Frame
Day 2
Title
Specificity of pulmonary ultrasound
Description
Proportion of subjects with a positive pulmonary ultrasound among those with a negative chest X-ray at time t at day 3
Time Frame
Day 3
Title
Sensitivity of pulmonary ultrasound in relation with ATS diagnosis
Description
Proportion of subjects with positive pulmonary ultrasound among those with a positive chest X-ray at time t with 95% confidence intervalat day -3 of ATS diagnosis
Time Frame
day -3 of ATS diagnosis
Title
Sensitivity of pulmonary ultrasound in relation with ATS diagnosis
Description
Proportion of subjects with positive pulmonary ultrasound among those with a positive chest X-ray at time t with 95% confidence interval at day -1 of ATS diagnosis
Time Frame
day -1 of ATS diagnosis
Title
Sensitivity of pulmonary ultrasound in relation with ATS diagnosis
Description
Proportion of subjects with positive pulmonary ultrasound among those with a positive chest X-ray at time t with 95% confidence interval at day -2 of ATS diagnosis
Time Frame
day -2 of ATS diagnosis
Title
Specificity of pulmonary ultrasound in relation with ATS diagnosis
Description
Proportion of subjects with a positive pulmonary ultrasound among those with a negative chest X-ray at time t at day -1 of ATS diagnosis
Time Frame
day -1 of ATS diagnosis
Title
Specificity of pulmonary ultrasound in relation with ATS diagnosis
Description
Proportion of subjects with a positive pulmonary ultrasound among those with a negative chest X-ray at time t at day -3 of ATS diagnosis
Time Frame
-3 day of ATS diagnosis
Title
Specificity of pulmonary ultrasound in relation with ATS diagnosis
Description
Proportion of subjects with a positive pulmonary ultrasound among those with a negative chest X-ray at time t at day -2 of ATS diagnosis
Time Frame
day -2 of ATS diagnosis
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Months
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age: ≥12 months and <18 years
Has a major sickle cell disease whatever the genotype
Admission to hospital for a febrile vaso-occlusive crisis (VOC) or not
Evolving at home for less than 48h
Concomitant treatment with hydroxycarbamide / hydroxyurea possible
Signed consent
Patients affiliated to a French social security scheme
Exclusion Criteria:
Child presenting an acute thoracic syndrome (ATS) from the outset at the admission
Child who presented an ATS in the month preceding the inclusion
Child in regular transfusion program or child who has received a hematopoietic stem cell transplant
Child hospitalized at least 5 times for VOC in the year preceding inclusion (psychic problems making difficult the evaluation of the pain)
Child who has already been included in the study during a previous VOC (each child participates in the study only once)
VOC evolving for more than 48 hours before admission to the emergency room
Acute splenic sequestration crisis at admission
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Camille JUNG, MD, PhD
Phone
+3357022268
Email
camille.jung@chicreteil.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Fouad MADHI, MD
Email
fouad.madhi@chicreteil.fr
Facility Information:
Facility Name
Hôpital Antoine Béclère
City
Clamart
ZIP/Postal Code
92141
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mélanie TAVEIRA, MD
Email
melanie.taveira@aphp.fr
Facility Name
Centre Hospitalier Intercommunal Créteil
City
Créteil
ZIP/Postal Code
94000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fouad MADHI, MD
Email
fouad.madhi@chicreteil.fr
Facility Name
Hôpital Bicêtre
City
Le Kremlin-Bicêtre
ZIP/Postal Code
94270
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Irina CRAIU, MD
Email
irina.craiu@aphp.fr
Facility Name
Hôpital Armand Trousseau
City
Paris
ZIP/Postal Code
75012
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Guillaume Thouvenin, MD
First Name & Middle Initial & Last Name & Degree
Céline Delestrain, MD
Email
celine.delestrain@aphp.fr
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Pulmonary Ultrasound in the Diagnosis of Acute Thoracic Syndrome in Vaso-occlusive Sickle Cell Crisis
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